Results 171 to 180 of about 2,774 (200)

Physical exercise in metabolic myopathies at risk of rhabdomyolysis: a feasible approach or an unavoidable hazard? [PDF]

Eur J Appl Physiol
Crisafulli O, Diotti D, Negro M, Lavaselli E, Peters M, Quintiero V, D'Antona G.   +6 more
europepmc   +1 more source

PDCD-DAT - a global database of pyroclastic density current deposit field data. [PDF]

J Appl Volcanol
Brown J, Williams R, Ogburn S, Brand B, Breard ECP, Charbonnier S, Dowey N, Dufek J, Jellinek M, Kueppers U, Lube G, Rowley P.   +11 more
europepmc   +1 more source

Phloridzin Mitigates Gorham-Stout Disease by Dual Inhibition of Osteoclastogenesis Related to the Ca²⁺ Signaling Pathway and Vascular Proliferation. [PDF]

ACS Omega
Trang NM, Kim EN, Jeong GS.
europepmc   +1 more source

Liver-Directed Gene Therapy Mitigates Early Nephropathy in Murine Glycogen Storage Disease Type Ia. [PDF]

J Inherit Metab Dis
Lee C, Pratap K, Zhang L, Chen HD, Arnaoutova I, Starost MF, Mansfield BC, Chou JY.   +7 more
europepmc   +1 more source

High-potency MyoAAV capsids enhanced skeletal muscle correction in a mouse model of GSD IIIa. [PDF]

Mol Ther Methods Clin Dev
Liao KA, Han SO, Barzi M, Yi H, Eisner W, Bissig-Choisat B, Bissig KD, Sun B.   +7 more
europepmc   +1 more source

Aesthetic Component of the Index of Orthodontic Treatment Need (IOTN): Can large language models match the performance of orthodontists? [PDF]

Korean J Orthod
Arısan A, Genҫ C, Duran GS.
europepmc   +1 more source

GSD Typ II und Typ IV: Biochemische und molekulargenetische Analyse bei Patienten mit Mangel an saurer α-Glukosidase bzw. mit Branchingenzymmangel

, 2005
Die Glykogen-Speicherkrankheit (GSD) ist eine seltene Stoffwechselerkrankung, die in verschiedenen Ausprägungen (Typen) vorkommt. Im ersten Teil der Arbeit wird durch Messung der Enzymaktivität von saurer α-Glukosidase und der Enzymaktivität des Branchingenzyms ein Screening-Test durchgeführt.
Lee, Hyun Kyung
openaire   +2 more sources

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Studies in Glycogen Storage Disease. IV. Leukocyte phosphorylase in a family with type VI GSD

Metabolism, 1970
Abstract A patient with Type VI Glycogen Storage Disease and members of his family have been studied utilizing leukocyte phosphorylase activities and erythrocyte glycogen levels to help elucidate the mode of inheritance of this disease. Leukocyte phosphorylase activities were found to be low in the patient, his clinically normal brother, parents ...
D, Schwartz, M, Savin, A, Drash, J, Field   +3 more
openaire   +2 more sources

SYSTEMIC PROGRESSION OF TYPE IV GLYCOGEN STORAGE DISEASE (GSD IV) AFTER LIVER TRANSPLANTATION (OLT)

Journal of Pediatric Gastroenterology and Nutrition, 1995
V Marchand, F Alvarez, A Rasquin‐Weber, H Blanchard, E Seidman, K Paradis   +5 more
openaire   +1 more source

A Mouse Model Of Adult Polyglucosan Body Disease (APBD), A Late Onset Variant Of Glycogen Storage Disease Type IV (GSD IV). (P1.054)

Neurology, 2014
Hasan Akman, Valentina Emmanuele, Sindu Krishna, Salvatore DiMauro   +3 more
openaire   +1 more source